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10.1007/s11033-022-07338-9

http://scihub22266oqcxt.onion/10.1007/s11033-022-07338-9
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35301654!8929466!35301654
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suck abstract from ncbi


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pmid35301654      Mol+Biol+Rep 2022 ; 49 (7): 6931-6943
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  • Differentially expressed plasmatic microRNAs in Brazilian patients with Coronavirus disease 2019 (COVID-19): preliminary results #MMPMID35301654
  • Nicoletti AS; Visacri MB; da Ronda CRDSC; Vasconcelos PEDNS; Quintanilha JCF; de Souza RN; Ventura DS; Eguti A; Silva LFS; Perroud Junior MW; Catharino RR; Reis LO; Dos Santos LA; Duran N; Favaro WJ; Lancellotti M; da Costa JL; Moriel P; Pincinato EC
  • Mol Biol Rep 2022[Jul]; 49 (7): 6931-6943 PMID35301654show ga
  • BACKGROUND: Coronavirus disease 2019 (COVID-19) is caused by a novel coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It is known that host microRNAs (miRNAs) can be modulated to favor viral infection or to protect the host. Herein, we report preliminary results of a study aiming at identifying differentially expressed plasmatic miRNAs in Brazilian patients with COVID-19. METHODS AND RESULTS: miRNAs were extracted from the plasma of eight patients with COVID-19 (four patients with mild COVID-19 and four patients with severe/critical COVID-19) and four healthy controls. Patients and controls were matched for sex and age. miRNA expression levels were detected using high-throughput sequencing. Differential miRNA expression and enrichment analyses were further evaluated. A total of 18 miRNAs were differentially expressed between patients with COVID-19 and controls. miR-4433b-5p, miR-6780b-3p, miR-6883-3p, miR-320b, miR-7111-3p, miR-4755-3p, miR-320c, and miR-6511a-3p were the most important miRNAs significantly involved in the PI3K/AKT, Wnt/beta-catenin, and STAT3 signaling pathways. Moreover, 42 miRNAs were differentially expressed between severe/critical and mild patients with COVID-19. miR-451a, miR-101-3p, miR-185-5p, miR-30d-5p, miR-25-3p, miR-342-3p, miR-30e-5p, miR-150-5p, miR-15b-5p, and miR-29c-3p were the most important miRNAs significantly involved in the Wnt/beta-catenin, NF-kappabeta, and STAT3 signaling pathways. CONCLUSIONS: If validated by quantitative real-time reverse transcriptase-polymerase chain reaction (RT-PCR) in a larger number of participants, the miRNAs identified in this study might be used as possible biomarkers for the diagnosis and severity of COVID-19.
  • |*COVID-19/genetics[MESH]
  • |*MicroRNAs/metabolism[MESH]
  • |Brazil/epidemiology[MESH]
  • |Gene Expression Profiling/methods[MESH]
  • |Humans[MESH]
  • |Phosphatidylinositol 3-Kinases/genetics[MESH]
  • |SARS-CoV-2[MESH]


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